🇺🇸 Vitamin E capsule in United States

10 US adverse-event reports

Safety signals — FAERS

Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.

• Window: 22 April 2025 – 22 April 2026
• Total reports: 10

Most-reported reactions

1. Alopecia — 1 report (10%)
2. Arthralgia — 1 report (10%)
3. Diarrhoea — 1 report (10%)
4. Dysgeusia — 1 report (10%)
5. Dyspepsia — 1 report (10%)
6. Dyspnoea — 1 report (10%)
7. Fatigue — 1 report (10%)
8. Feeling Abnormal — 1 report (10%)
9. Hallucination — 1 report (10%)
10. Pain — 1 report (10%)

Source database →

Frequently asked questions

Is Vitamin E capsule approved in United States?

Vitamin E capsule does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Vitamin E capsule in United States?

Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh is the originator. The local marketing authorisation holder may differ — check the official source linked above.